# FDA Inspection 854364 - Maquet Cardiopulmonary Ag - September 26, 2013

Source: https://www.keypedia.com/records/fda_inspections/maquet-cardiopulmonary-ag/3a1d629b-32ba-4304-9a5e-aa1db1ef9caa
Source feed: FDA_Inspections

> FDA Inspection 854364 for Maquet Cardiopulmonary Ag on September 26, 2013. Classification: Official Action Indicated (OAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 854364
- Company Name: Maquet Cardiopulmonary Ag
- Inspection Date: 2013-09-26
- Classification: Official Action Indicated (OAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1170411 - 2022-04-28](https://www.keypedia.com/records/fda_inspections/maquet-cardiopulmonary-ag/f5329199-7456-4276-9315-796c3d520079)
- [FDA Inspection 854364 - 2013-09-26](https://www.keypedia.com/records/fda_inspections/maquet-cardiopulmonary-ag/d253995d-bf10-49db-9ba4-a649ac9db381)

Company: https://www.keypedia.com/companies/maquet-cardiopulmonary-ag/da47333e-1cc7-4d68-aabf-c9743cdfd0f7

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7